Michael G DeGroote School of Medicine, McMaster University, Hamilton, Ontario, Canada.
McMaster University, Hamilton Health Sciences, Hamilton, Ontario, Canada.
Clin Breast Cancer. 2022 Oct;22(7):629-633. doi: 10.1016/j.clbc.2022.07.004. Epub 2022 Jul 11.
Metastatic HER2-positive (HER2+) and triple-negative breast cancer (TNBC) confer a 30% or higher risk of developing brain metastases (BrM), but BrM is typically an exclusion criteria for clinical trials, which limits the generalizability of trial results to these patients. We therefore analysed trends in the enrollment of patients with BrM, as well as the use of outcomes specific to the central nervous system (CNS), in phase III clinical trials evaluating systemic therapy for patients with advanced HER2+ and/or TNBC. Notably, 10 of the 34 trials (29%, 95% confidence interval = 15.1%-47.5%) evaluated CNS-specific outcomes and trials that completely excluded patients with BrM were significantly less likely to meet their primary endpoint (n = 6/17, 35%) than those that permitted conditional enrollment (n = 13/15, 87%) (P = .005), suggesting that enrollment of patients with BrM is not detrimental to trial success.
转移性人表皮生长因子受体 2 阳性(HER2+)和三阴性乳腺癌(TNBC)发生脑转移(BrM)的风险为 30%或更高,但 BrM 通常是临床试验的排除标准,这限制了试验结果在这些患者中的普遍性。因此,我们分析了入组 BrM 患者的趋势,以及在评估晚期 HER2+和/或 TNBC 患者系统治疗的 III 期临床试验中使用针对中枢神经系统(CNS)的结局的情况。值得注意的是,在评估 CNS 特异性结局的 34 项试验中有 10 项(29%,95%置信区间为 15.1%-47.5%),而完全排除 BrM 患者的试验显著不太可能达到主要终点(n=6/17,35%),而允许有条件入组的试验(n=13/15,87%)(P=0.005),这表明入组 BrM 患者不会对试验成功产生不利影响。